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2-Methylresorcinol → 2,4-Dihydroxy-3-methylbenzaldehyde

HRID 55714
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HRID 55714 반응식
P(Cl)(Cl)(Cl)=O.CN([CH:14]=[O:15])C1C=CC=CC=1.[CH3:16][C:17]1[C:23]([OH:24])=[CH:22][CH:21]=[CH:20][C:18]=1[OH:19]>CCOCC>[OH:19][C:18]1[C:17]([CH3:16])=[C:23]([OH:24])[CH:22]=[CH:21][C:20]=1[CH:14]=[O:15]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 118432-MethylresorcinolHCID 24813Phosphorus oxychlorideHCID 66737N-Methylformanilide

생성물 1

HCID 803952,4-Dihydroxy-3-methylbenzaldehyde수율 57%

시약·촉매·용매 1

HCID 3283Diethyl Ether용매

실험 절차

Phosphorus oxychloride (80 mL, 0.86 mol) was added to a stirred mixture of N-methylformanilide (102 mL, 0.82 mol) in ether (250 mL). The mixture was stirred for 1 hour at room temperature and then cooled in ice. 2-Methyl resorcinol (Aldrich, 100 g, 0.81 mol) was added and the mixture was allowed to warm to room temperature while stirring overnight. The precipitated intermediate product was collected by filtration and rinsed with ether (3×). The intermediate was hydrolyzed by dissolving in a mixture of acetone (250 mL) and water (250 mL) and stirring for 30 minutes. Water (2 L) was added, the mixture was brought to a boil, and then allowed to cool and deposit crystalline product. This was recrystallized a second time from water (4 L) to afford pure product (70 g, 57%). M.p. 150° C. (Lit. 152°-3° C. [W. Baker et al., J. Chem. Soc. 2834-5 (1949)⟧

후처리

  1. temperaturecooled in ice
  2. temperatureto warm to room temperature
  3. stirringwhile stirring overnight
  4. filtrationThe precipitated intermediate product was collected by filtration
  5. washrinsed with ether (3×)
  6. dissolutionby dissolving in a mixture of acetone (250 mL) and water (250 mL)
  7. stirringstirring for 30 minutes
  8. additionWater (2 L) was added
  9. temperatureto cool
  10. customThis was recrystallized a second time from water (4 L)

출처 및 근거

ORD 기록
ord-2272eae45ce6481684641bd9ff2d287f
출처 데이터셋
uspto-grants-1997_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05625081

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